Analysis of blockwise shrinkage wavelet estimates via lower bounds for no-signal setting

A blockwise shrinkage is a popular procedure of adaptation that has allowed the statisticians to establish an impressive bouquet of asymptotic mathematical results and develop softwares for solving practical problems. Traditionally risks of the estimates are studied via upper bounds that imply sufficient conditions for a blockwise shrinkage procedure to be minimax. This article suggests to analyze the estimates via exact (non-asymptotic) lower bounds established for a no-signal setting. The approach complements the familiar minimax, Bayesian and numerical analysis, it allows to find necessary conditions for a procedure to attain desired rates, and it sheds a new light on popular choices of blocks and thresholds recommended in the literature. Mathematical results are complemented by a numerical study. Supported in part by NSF Grants DMS-9971051 and DMS-0243606.     

Sample path analysis of level crossings for the workload process

We examine level crossings of sample paths of queueing processes and investigate the conditions under which the limiting empirical distribution for the workload process exists and is absolutely continuous. The connection between the density of the workload distribution and the rate of downcrossings is established as a sample path result that does not depend on any stochastic assumptions. As a corollary, we obtain the sample path version of the Takács formula connecting the time and customer stationary distributions in a queue. Defective limiting empirical distributions are considered and an expression for the mass at infinity is derived.This research has been supported in part by NSF Grants ECS-8811003 and DDM-8905638.     

嵌套病例对照研究中的两步估计方法（英）

本文讨论嵌套病例对照研究中相对危险率的估计问题，引入了相对危险率的两步估计，并在一般嵌套病例对照抽样的假设下讨论了相对危险率的两步估计的相合性问题，最后给出了几个例子。     

Template atom transfer radical polymerization of a diaminopyrimidine‐derivatized monomer in the presence of a uracil‐containing polymer

Uracil‐derivatized monomer 6‐undecyl‐1‐(4‐vinylbenzyl)uracil and diaminopyrimidine‐derivatized monomer 2,6‐dioctanoylamido‐4‐methacryloyloxypyrimidine (DMP) were synthesized and polymerized by atom transfer radical polymerization (ATRP). A well‐defined, highly soluble, uracil‐containing polymer, poly[6‐undecyl‐1‐(4‐vinylbenzyl)uracil] (PUVU), was prepared in dioxane at 90 °C with CuBr/1,1,4,7,10,10‐hexamethyltriethylenetetramine as the catalyst and methyl α‐bromophenylacetate as the initiator. PUVU was further used as a template for the ATRP of DMP. The enhanced apparent rate constant of the DMP polymerization in the presence of PUVU indicated that the ATRP of DMP occurred along the PUVU template. The template polymerization produced a stable and insoluble macromolecular complex, PUVU/poly(2,6‐dioctanoylamido‐4‐methacryloyloxypyrimidine). An X‐ray diffraction study confirmed that the complex had strandlike domains. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6607–6615, 2006     

Effect of the environment on the stability of surfactant–polypeptide self‐assembled complexes: Molecular dynamics simulations of stoichiometric complexes formed by N‐dodecyltrimethylammonium and poly(α,L‐glutamate) in chloroform,methanol, and water

A series of molecular dynamics simulations have been performed to study the supramolecular structure of self‐assembled complexes formed by N‐dodecyltrimethylammonium cations and the synthetic polypeptide poly(α,L ‐glutamate). The influence of the type of solvent has been investigated, considering explicit environments of chloroform, water, and methanol on a stoichiometric complex containing 15 residues. In chloroform, the complex stabilizes in a regular structure: the polypeptide adopts an α‐helix conformation that is regularly surrounded by surfactant molecules to form electrostatic interactions through a multiple interaction pattern. However, this structure destabilizes in methanol and water: (a) the α‐helix unfolds in the two solvents and (b) the electrostatic links between the surfactant molecules and the polyanion are disrupted in aqueous solution, although these interactions are still preserved in methanol. The role of the solvent environment in stabilizing or destabilizing the polypeptide secondary structure, the organization of the surfactant molecules, and predominantly the surfactant–polypeptide supramolecular organization is discussed in detail. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1122–1133, 2006     

液相色谱法测定地质样品中的芳香化合物

发展了用液相色谱法检测地质样品中芳香化合物的方法。对观察到的色谱峰进行了定性分析，了该法对油气地球化学勘探的意义。     

固体基质室温燐光法测定L-色氨酸

本文提出在Na_2 CO_3存在下,以NaI为重原子微扰剂,以滤纸为基质的L-色氨酸的室温燐光(RTP)测定法。本法不需通干燥气体,工作曲线的线性范围较宽,用于谷物试样分析,得到了满意的结果。